Ingo Mellinghoff
· ProfessorCornell University · Pharmacology and Chemical Biology
Active 1991–2026
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About
Ingo Mellinghoff, MD, FACP, is a physician-scientist whose laboratory focuses on the study of molecular pathways that regulate brain tumor growth. His long-term goal is to develop therapeutic paradigms that target specific properties of primary brain tumors, including genetic alterations in cancer signaling pathways, unique aspects of brain tumor metabolism, and interactions of brain tumor cells with their brain microenvironment. His research involves studies in experimental brain tumor models that are closely linked to the evaluation of novel agents in early-phase clinical trials. Dr. Mellinghoff has contributed to significant advancements in the treatment of low-grade gliomas, including the development and clinical testing of targeted drugs such as vorasidenib and ivosidenib, which reduce tumor-associated metabolites and show encouraging tumor responses. His work has led to the FDA approval of drugs for low-grade glioma with IDH gene mutations and has been published in high-impact journals. His research also explores the use of liquid biopsies from spinal fluid to guide brain tumor diagnosis and treatment, and he has been involved in studies tracking tumor evolution through cerebrospinal fluid analysis.
Research topics
- Internal medicine
- Oncology
- Medicine
- Cancer research
- Pathology
- Biology
- Engineering
- Genetics
- Intensive care medicine
- Medical physics
Selected publications
Glioblastoma and Other Primary Brain Malignancies in Adults
JAMA · 2023 · 1129 citations
Senior authorCorrespondingImportance: Malignant primary brain tumors cause more than 15 000 deaths per year in the United States. The annual incidence of primary malignant brain tumors is approximately 7 per 100 000 individuals and increases with age. Five-year survival is approximately 36%. Observations: Approximately 49% of malignant brain tumors are glioblastomas, and 30% are diffusely infiltrating lower-grade gliomas. Other malignant brain tumors include primary central nervous system (CNS) lymphoma (7%) and malignan…
Neuro-Oncology · 2020 · 1111 citations
Glioblastomas are the most common form of malignant primary brain tumor and an important cause of morbidity and mortality. In recent years there have been important advances in understanding the molecular pathogenesis and biology of these tumors, but this has not translated into significantly improved outcomes for patients. In this consensus review from the Society for Neuro-Oncology (SNO) and the European Association of Neuro-Oncology (EANO), the current management of isocitrate dehydrogenase w…
Vorasidenib in IDH1- or IDH2-Mutant Low-Grade Glioma
New England Journal of Medicine · 2023 · 683 citations
1st authorCorrespondingBACKGROUND: Isocitrate dehydrogenase (IDH)-mutant grade 2 gliomas are malignant brain tumors that cause considerable disability and premature death. Vorasidenib, an oral brain-penetrant inhibitor of mutant IDH1 and IDH2 enzymes, showed preliminary activity in IDH-mutant gliomas. METHODS: In a double-blind, phase 3 trial, we randomly assigned patients with residual or recurrent grade 2 IDH-mutant glioma who had undergone no previous treatment other than surgery to receive either oral vorasidenib…
Journal of Clinical Oncology · 2023 · 47 citations
PURPOSE: The Individualized Screening Trial of Innovative Glioblastoma Therapy (INSIGhT) is a phase II platform trial that uses response adaptive randomization and genomic profiling to efficiently identify novel therapies for phase III testing. Three initial experimental arms (abemaciclib [a cyclin-dependent kinase [CDK]4/6 inhibitor], neratinib [an epidermal growth factor receptor [EGFR]/human epidermal growth factor receptor 2 inhibitor], and CC-115 [a deoxyribonucleic acid-dependent protein k…
Neuro-Oncology · 2022 · 23 citations
Imaging response assessment is a cornerstone of patient care and drug development in oncology. Clinicians/clinical researchers rely on tumor imaging to estimate the impact of new treatments and guide decision making for patients and candidate therapies. This is important in brain cancer, where associations between tumor size/growth and emerging neurological deficits are strong. Accurately measuring the impact of a new therapy on tumor growth early in clinical development, where patient numbers a…
Recent grants
Molecular Mechanisms of IDH1-mediated Gliomagenesis
NIH · $411k · 2012–2017
Molecular Mechanisms of IDH1-mediated Gliomagenesis
NIH · $1.6M · 2012–2018
Molecular Mechanisms of Drug Resistance in Primary Brain Tumors
NIH · $4.7M · 2018–2025
Frequent coauthors
- 442 shared
Patrick Y. Wen
- 428 shared
Timothy F. Cloughesy
University of California, Los Angeles
- 284 shared
Carl Campos
Memorial Sloan Kettering Cancer Center
- 251 shared
Michael D. Prados
University of California, San Francisco
- 241 shared
Lisa M. DeAngelis
Memorial Sloan Kettering Cancer Center
- 205 shared
Paul S. Mischel
Stanford University
- 172 shared
Cameron Brennan
- 172 shared
John G. Kuhn
University of California, Los Angeles
Labs
The Ingo Mellinghoff LabPI
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